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6319-32-0

4-chloro-3-phenylquinoline is a heterocyclic chemical compound with the molecular formula C16H10ClN. It features a quinoline core, which is a tricyclic system with a chlorine atom at the 4th position and a phenyl group attached at the 3rd position. 4-chloro-3-phenylquinoline has garnered attention in the fields of organic and medicinal chemistry due to its intriguing pharmacological properties and potential as a molecular scaffold for developing drugs and biologically active compounds.

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  • 6319-32-0 Structure

  • Basic information

    1. Product Name: 4-chloro-3-phenylquinoline
    2. Synonyms:
    3. CAS NO:6319-32-0
    4. Molecular Formula: C15H10ClN
    5. Molecular Weight: 239.6996
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6319-32-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 355.3°C at 760 mmHg
    3. Flash Point: 199.8°C
    4. Appearance: N/A
    5. Density: 1.235g/cm3
    6. Vapor Pressure: 6.46E-05mmHg at 25°C
    7. Refractive Index: 1.66
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-chloro-3-phenylquinoline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-chloro-3-phenylquinoline(6319-32-0)
    12. EPA Substance Registry System: 4-chloro-3-phenylquinoline(6319-32-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6319-32-0(Hazardous Substances Data)

6319-32-0 Usage

Uses

Used in Pharmaceutical Industry:
4-chloro-3-phenylquinoline is utilized as a molecular scaffold for the development of new drugs and biologically active compounds. Its unique structure and properties make it a promising candidate for researchers working on the design and synthesis of novel chemical entities aimed at treating various diseases and medical conditions.
Used in Organic Chemistry Research:
In the realm of organic chemistry, 4-chloro-3-phenylquinoline serves as a subject of interest for scientists exploring the synthesis and modification of heterocyclic compounds. Its potential applications in creating new chemical entities for various industries, including pharmaceuticals, make it a valuable compound for ongoing research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 6319-32-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6319-32:
(6*6)+(5*3)+(4*1)+(3*9)+(2*3)+(1*2)=90
90 % 10 = 0
So 6319-32-0 is a valid CAS Registry Number.

6319-32-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-3-phenylquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,4-chloro-3-phenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6319-32-0 SDS

6319-32-0Relevant articles and documents

Azaisoflavones: Synthesis, antimicrobial evaluation and binding affinity with DNA gyrase

Praveen,Parthasarathy,Kumar, P. Senthil,Perumal

, p. 373 - 382 (2015/03/31)

Antimicrobial potency of azaisoflavones has been evaluated in vitro against nine bacterial and two fungal strains, respectively. The requisite azaisoflavones are conveniently synthesized in three steps, with the key step being the super acid catalyzed tandem reaction. The biological results reveal that out of twelve compounds screened, 3 compounds (5a, 5j and 5l) exhibited comparable activities against the standard drugs and demonstrated activities at μM concentration. In addition, molecular docking revealed that compound 5a as the most potent by showing a least binding energy of -5.99 kcal/mol with DNA gyrase receptor compared to other compounds.

C-H arylation of pyridines: High regioselectivity as a consequence of the electronic character of C-H bonds and heteroarene ring

Guo, Pengfei,Joo, Jung Min,Rakshit, Souvik,Sames, Dalibor

supporting information; experimental part, p. 16338 - 16341 (2011/11/29)

We report a new catalytic protocol for highly selective C-H arylation of pyridines containing common and synthetically versatile electron-withdrawing substituents (NO2, CN, F and Cl). The new protocol expands the scope of catalytic azine functi

Synthesis of 4-Aryl-2-aminopyridine derivatives and related compounds

Pavlovic, Vladimir,Petkovic, Milos,Popovic, Stanimir,Savic, Vladimir

experimental part, p. 4249 - 4263 (2010/01/15)

A short, efficient, and high-yielding synthesis of 4-aryl-2-aminopyridine derivatives has been developed. The route employs two palladium-catalyzed processes, the Suzuki reaction and the Buchwald-Hartwig amination, as the key steps. The same approach has

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